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2-(3-Methyl-morpholin-4-yl)-ethylamine | 1154940-86-9

中文名称
——
中文别名
——
英文名称
2-(3-Methyl-morpholin-4-yl)-ethylamine
英文别名
2-(3-Methylmorpholin-4-yl)ethan-1-amine;2-(3-methylmorpholin-4-yl)ethanamine
2-(3-Methyl-morpholin-4-yl)-ethylamine化学式
CAS
1154940-86-9
化学式
C7H16N2O
mdl
MFCD12134211
分子量
144.217
InChiKey
AKRYVGKRXDTOBA-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    213.2±20.0 °C(Predicted)
  • 密度:
    0.962±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.6
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    38.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    3-氯-4-甲基-6-苯基哒嗪2-(3-Methyl-morpholin-4-yl)-ethylamine 生成 4-methyl-N-[2-(3-methylmorpholin-4-yl)ethyl]-6-phenylpyridazin-3-amine,dihydrochloride
    参考文献:
    名称:
    3-Aminopyridazine derivatives with atypical antidepressant, serotonergic and dopaminergic activities
    摘要:
    Minaprine [3-[(beta-morpholinoethyl)amino]-4-methyl-6-phenylpyridazine dihydrochloride] is active in most animal models of depression and exhibits in vivo a dual dopaminomimetic and serotoninomimetic activity profile. In an attempt to dissociate these two effects and to characterize the responsible structural requirements, a series of 47 diversely substituted analogues of minaprine were synthesized and tested for their potential antidepressant, serotonergic, and dopaminergic activities. The structure-activity relationships show that dopaminergic and serotonergic activities can be dissociated. Serotonergic activity appears to be correlated mainly with the substituent in the 4-position of the pyridazine ring whereas the dopaminergic activity appears to be dependent on the presence, or in the formation, of a para-hydroxylated aryl ring in the 6-position of the pyridazine ring.
    DOI:
    10.1021/jm00123a004
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文献信息

  • KASZTREINER, E.;RABLOCZKY, G.;MAKK, N.;MATYUS, P.;DIESLER, E.;TEGDES, A.;+, EUR. J. MED. CHEM., 25,(1990) N, C. 333-341
    作者:KASZTREINER, E.、RABLOCZKY, G.、MAKK, N.、MATYUS, P.、DIESLER, E.、TEGDES, A.、+
    DOI:——
    日期:——
  • US4992150A
    申请人:——
    公开号:US4992150A
    公开(公告)日:1991-02-12
  • 3-Aminopyridazine derivatives with atypical antidepressant, serotonergic and dopaminergic activities
    作者:Camille Georges Wermuth、Gilbert Schlewer、Jean Jacques Bourguignon、Georges Maghioros、Marie Jeanne Bouchet、Claudine Moire、Jean Paul Kan、Paul Worms、Kathleen Biziere
    DOI:10.1021/jm00123a004
    日期:1989.3
    Minaprine [3-[(beta-morpholinoethyl)amino]-4-methyl-6-phenylpyridazine dihydrochloride] is active in most animal models of depression and exhibits in vivo a dual dopaminomimetic and serotoninomimetic activity profile. In an attempt to dissociate these two effects and to characterize the responsible structural requirements, a series of 47 diversely substituted analogues of minaprine were synthesized and tested for their potential antidepressant, serotonergic, and dopaminergic activities. The structure-activity relationships show that dopaminergic and serotonergic activities can be dissociated. Serotonergic activity appears to be correlated mainly with the substituent in the 4-position of the pyridazine ring whereas the dopaminergic activity appears to be dependent on the presence, or in the formation, of a para-hydroxylated aryl ring in the 6-position of the pyridazine ring.
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